(S)-(+)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID CAS 21461-84-7

Introduction:Basic information about (S)-(+)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID CAS 21461-84-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

(S)-(+)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID Basic information

Product Name:(S)-(+)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID
Synonyms:5-OXO-2-TETRAHYDROFURANCARBOXYLIC ACID (S-);5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID;(S)-(+)-GAMMA-CARBOXY-GAMMA-BUTYROLACTONE;(S)-GAMMA-CARBOXY-GAMMA-BUTYROLACTONE;(S)-(+)-TETRAHYDRO-5-OXO-2-FURANCARBOXYLIC ACID;(S)-(+)-TETRAHYDRO-5-OXO-2-FURANECARBOXYLIC ACID;TIMTEC-BB SBB006581;(S)-(+)-5-OXO-2-TETRAHYDROFURANCARBOXYLIC ACID
CAS:21461-84-7
MF:C5H6O4
MW:130.1
EINECS:
Product Categories:Carboxylic Acids (Chiral);Chiral Building Blocks;Synthetic Organic Chemistry;Chiral Reagents;Miscellaneous Reagents
Mol File:21461-84-7.mol

(S)-(+)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID Chemical Properties

Melting point 71-73 °C (lit.)
alpha +14°(20/D, c=5, CH3OH)
Boiling point 150-155 °C/0.2 mmHg (lit.)
density 1.3985 (rough estimate)
refractive index 1.5800 (estimate)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Acetone
form Solid
pka3.11±0.20(Predicted)
color White
Optical Rotation[α]20/D +14°, c = 5 in methanol
BRN 1424498
InChIInChI=1S/C5H6O4/c6-4-2-1-3(9-4)5(7)8/h3H,1-2H2,(H,7,8)/t3-/m0/s1
InChIKeyQVADRSWDTZDDGR-VKHMYHEASA-N
SMILESO1C(=O)CC[C@H]1C(O)=O
CAS DataBase Reference21461-84-7(CAS DataBase Reference)

Safety Information

Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 29321900
Storage Class11 - Combustible Solids

(S)-(+)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID Usage And Synthesis

Chemical Propertieswhite to light yellow to beige crystalline powder
Uses(S)-5-Oxo-2-tetrahydrofurancarboxylic Acid (cas# 21461-84-7) is a compound useful in organic synthesis.
DefinitionChEBI: (S)-alpha-hydroxyglutaric acid-gamma-lactone is a butan-4-olide obtained by formal intramolecular condensation between the 2-hydroxy and 4-carboxy groups of (S)-2-hydroxyglutaric acid It is a butan-4-olide and a monocarboxylic acid. It is functionally related to a (S)-2-hydroxyglutaric acid. It is a conjugate acid of a (S)-alpha-hydroxyglutarate-gamma-lactone.
General Description(S)-(+)-5-Oxo-2-tetrahydrofurancarboxylic acid is a chiral derivatizing agent for alcohols.
Synthesis

56-86-0

21461-84-7

General procedure for the synthesis of (S)-5-oxo-2-tetrahydrofuran carboxylic acid from L-glutamic acid: L-glutamic acid (10.07 g, 0.068 mol, JK CHEMICA) was dissolved in 20 mL of water in a conical flask. A solution of NaNO2 (7.0 g, 0.102 mol, Shantou Xilong Chemical Factory) in 20 mL of water was slowly added to this solution at -5°C, along with HCl and 40 mL of water. The reaction mixture was stirred continuously at room temperature for 12 hours. Subsequently, the reaction mixture was subjected to vacuum evaporation at less than 50 °C to obtain a yellow oily substance. This oily substance was dissolved in EtOAc, filtered to remove the solid formed and the solid was washed with EtOAc. The filtrate and washings were combined and dried with Na2SO4. Finally, the solvent was removed by vacuum concentration to afford (S)-5-oxo-2-tetrahydrofuran carboxylic acid as a light yellow oil (8.1 g, 91.6% yield). The product was analyzed by mass spectrometry (ESI, cation mode), m/z: 130.9 (M+1); 1H NMR (400 MHz, CDCl3) data were as follows: δ 2.27-2.41 (m, 1H), 2.44-2.65 (m, 3H), 5.09 (m, 1H), 9.12-9.55 (m, 1H).

References[1] Journal of Organic Chemistry, 2010, vol. 75, # 2, p. 390 - 398
[2] Patent: WO2010/45095, 2010, A1. Location in patent: Page/Page column 69; 70
[3] Synthesis, 2007, # 15, p. 2279 - 2286
[4] Tetrahedron, 2009, vol. 65, # 48, p. 9997 - 10001
[5] Carbohydrate Research, 1983, vol. 124, p. 35 - 42

(S)-(+)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID Preparation Products And Raw materials

Raw materialsHydrochloric acid-->Ethyl acetate-->Tetrahydrofuran-->PETROLEUM ETHER-->Sodium nitrite-->Benzene-->L-Glutamic acid
Preparation Products(S)-5-Hydroxymethyldihydrofuran-2-one
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